Double-Blind Study
Definition
A clinical trial design where neither the participants nor the researchers know who is receiving the active drug versus placebo. Double-blinding prevents both patient expectations and researcher bias from influencing the results.
Beispiel
In a double-blind antidepressant trial, identical-looking pills are used so that neither patients nor doctors can distinguish the active drug from the placebo.
Verwandte Begriffe
In Leitfäden Erwähnt
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